TY - JOUR
T1 - Erratum
T2 - Photodissociation of the Product from a Transition-Metal Center Allows the Catalytic Cycle to Proceed: The Rhodium(I)-Catalyzed [2+2+1] Carbonylative Cycloaddition of Diynes (Organic Letters (2021) 23:12 (4893-4897) DOI: 10.1021/acs.orglett.1c01631)
AU - Jia, Jing Wen
AU - Morimoto, Tsumoru
AU - Yamaguchi, Yoshiko
AU - Tanimoto, Hiroki
AU - Kakiuchi, Kiyomi
N1 - Publisher Copyright:
© 2022 American Chemical Society.
PY - 2022/1/21
Y1 - 2022/1/21
N2 - In the Supporting Information for the paper (ol1c01631_si_001), NMR charts of compounds 2a, 2c, 2d, and 2e were from materials synthesized by a previous procedure:1 compound 2a 1H NMR (page S50); compound 2c 1H NMR (page S54); compound 2d 1H and 13C NMRs (pages S56 and S57); compound 2e 1H NMR (page S58). The respective NMR charts of these products in the Supporting Information have been replaced with those obtained from the reactions reported in this paper (2a, page S52; 2c, page S56; 2d, pages S58 and S59). For the product 2e, since the primary FID files of both its 1H and 13C NMR have been lost, the charts have been replaced with newly acquired spectra (pages S60 and S61) obtained from a new trial with 1e which showed similar yield as reported initially (9.4% yield of 2e). The primary NMR FID files for all the products, including the above ones, have been uploaded. These revisions do not change the analysis, discussion, and conclusion in the original paper.
AB - In the Supporting Information for the paper (ol1c01631_si_001), NMR charts of compounds 2a, 2c, 2d, and 2e were from materials synthesized by a previous procedure:1 compound 2a 1H NMR (page S50); compound 2c 1H NMR (page S54); compound 2d 1H and 13C NMRs (pages S56 and S57); compound 2e 1H NMR (page S58). The respective NMR charts of these products in the Supporting Information have been replaced with those obtained from the reactions reported in this paper (2a, page S52; 2c, page S56; 2d, pages S58 and S59). For the product 2e, since the primary FID files of both its 1H and 13C NMR have been lost, the charts have been replaced with newly acquired spectra (pages S60 and S61) obtained from a new trial with 1e which showed similar yield as reported initially (9.4% yield of 2e). The primary NMR FID files for all the products, including the above ones, have been uploaded. These revisions do not change the analysis, discussion, and conclusion in the original paper.
UR - http://www.scopus.com/inward/record.url?scp=85123522378&partnerID=8YFLogxK
U2 - 10.1021/acs.orglett.1c03854
DO - 10.1021/acs.orglett.1c03854
M3 - コメント/討論
C2 - 34978194
AN - SCOPUS:85123522378
SN - 1523-7060
VL - 24
SP - 797
JO - Organic Letters
JF - Organic Letters
IS - 2
ER -